SEARCH RESULTS for: 5K3991GVWI (15 results)

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AUSTEDO (DEUTETRABENAZINE) TABLET, COATED AUSTEDO (DEUTETRABENAZINE) KIT AUSTEDO XR (DEUTETRABENAZINE) TABLET, FILM COATED, EXTENDED RELEASE

NDC Code(s): 68546-161-15, 68546-163-15, 68546-165-15, 68546-170-60, view more
68546-170-66, 68546-171-60, 68546-171-66, 68546-172-60, 68546-172-66, 68546-176-28, 68546-177-21, 68546-181-49, 68546-182-70, 68546-470-56, 68546-471-56, 68546-472-56, 68546-490-42, 68546-490-52
• Packager: TEVA NEUROSCIENCE, INC.

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METHYLPHENIDATE HYDROCHLORIDE TABLET, EXTENDED RELEASE

NDC Code(s): 43598-438-01, 43598-439-01, 43598-440-01, 43598-441-01
• Packager: DR.REDDYS LABORATORIES INC

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PREGABALIN TABLET, FILM COATED, EXTENDED RELEASE

NDC Code(s): 72888-049-30, 72888-050-30, 72888-051-30
• Packager: ADVAGEN PHARMA LTD.

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PREGABALIN TABLET, FILM COATED, EXTENDED RELEASE

NDC Code(s): 69986-013-01, 69986-014-01, 69986-015-01
• Packager: SINOTHERAPEUTICS INC.

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MIRABEGRON TABLET, EXTENDED RELEASE

NDC Code(s): 70771-1752-1, 70771-1752-3, 70771-1752-9, 70771-1753-1, view more
70771-1753-3, 70771-1753-9
• Packager: ZYDUS LIFESCIENCES LIMITED

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MIRABEGRON TABLET, EXTENDED RELEASE

NDC Code(s): 70710-1159-1, 70710-1159-3, 70710-1159-9, 70710-1160-1, view more
70710-1160-3, 70710-1160-9
• Packager: ZYDUS PHARMACEUTICALS (USA) INC.

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MYRBETRIQ (MIRABEGRON) TABLET, FILM COATED, EXTENDED RELEASE MYRBETRIQ (MIRABEGRON) GRANULE, FOR SUSPENSION, EXTENDED RELEASE

NDC Code(s): 0469-2601-07, 0469-2601-30, 0469-2601-90, 0469-2602-07, view more
0469-2602-30, 0469-2602-90, 0469-5020-99
• Packager: ASTELLAS PHARMA US, INC.

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BUPRENORPHINE AND NALOXONE FILM

NDC Code(s): 50742-364-01, 50742-364-30, 50742-365-01, 50742-365-30
• Packager: INGENUS PHARMACEUTICALS, LLC

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MYRBETRIQ (MIRABEGRON) TABLET, FILM COATED, EXTENDED RELEASE

NDC Code(s): 70518-2435-0, 70518-2435-1, 70518-2435-2, 70518-2435-3, view more
70518-2435-4
• Packager: REMEDYREPACK INC.
• This is a repackaged label.
• Source NDC Code(s): 0469-2602

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MYRBETRIQ (MIRABEGRON) TABLET, FILM COATED, EXTENDED RELEASE

NDC Code(s): 70518-3158-0, 70518-3158-1, 70518-3158-2, 70518-3158-3
• Packager: REMEDYREPACK INC.
• This is a repackaged label.
• Source NDC Code(s): 0469-2601

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OUAI ANTI-DANDRUFF (SALICYLIC ACID) SHAMPOO

NDC Code(s): 83058-0140-1, 83058-0140-4
• Packager: UNITED BEAUTY BRANDS, LLC

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BUPROPION HYDROCHLORIDE TABLET, FILM COATED, EXTENDED RELEASE

NDC Code(s): 24979-248-06
• Packager: TWI PHARMACEUTICALS, INC.

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FORFIVO XL (BUPROPION HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE

NDC Code(s): 52427-575-30
• Packager: ALMATICA PHARMA INC.

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BUPROPION HYDROCHLORIDE TABLET, FILM COATED, EXTENDED RELEASE

NDC Code(s): 47781-637-30
• Packager: ALVOGEN INC.

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FORFIVO XL (BUPROPION HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE

NDC Code(s): 24979-247-06
• Packager: TWI PHARMACEUTICALS, INC.